EP0284560B1 - Colorants de dispersion contenant un groupement tricyanovinyle - Google Patents

Colorants de dispersion contenant un groupement tricyanovinyle Download PDF

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Publication number
EP0284560B1
EP0284560B1 EP88810156A EP88810156A EP0284560B1 EP 0284560 B1 EP0284560 B1 EP 0284560B1 EP 88810156 A EP88810156 A EP 88810156A EP 88810156 A EP88810156 A EP 88810156A EP 0284560 B1 EP0284560 B1 EP 0284560B1
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Prior art keywords
formula
dye
hydrogen
dye according
c4alkoxy
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EP88810156A
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German (de)
English (en)
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EP0284560A2 (fr
EP0284560A3 (en
Inventor
Peter Dr. Liechti
Angelo Della Casa
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Novartis AG
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Ciba Geigy AG
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
    • C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
    • C09B67/008—Preparations of disperse dyes or solvent dyes
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B23/00—Methine or polymethine dyes, e.g. cyanine dyes
    • C09B23/14—Styryl dyes
    • C09B23/143—Styryl dyes the ethylene chain carrying a COOH or a functionally modified derivative, e.g.-CN, -COR, -COOR, -CON=, C6H5-CH=C-CN
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
    • C09B56/00—Azo dyes containing other chromophoric systems
    • C09B56/08—Styryl-azo dyes

Definitions

  • the present invention relates to disperse dyes, processes for their preparation and their use for dyeing synthetic organic material.
  • the dyes according to the invention correspond to the formula wherein X is hydrogen, C1-C4-alkyl, C1-C4-alkoxy or halogen, Y is hydrogen, halogen, C1-C4-alkyl, C1-C4-alkoxy, C1-C4-alkoxy-C1-C4-alkyl or C1-C4-alkoxy-C1-C4-alkoxy, R is hydrogen, C1-C12-alkyl, C2-C12-alkenyl or phenyl, or Y and R, together with the nitrogen atom and the two C atoms connecting them, form a 5- or 6-ring, B is a straight-chain or branched C2-C6 alkylene radical, Z is a bridge member of the formula -O-, -S-, -NH-, or a direct bond and A is a residue of the formula means, these radicals can also be substituted by C1-C4-alkyl, C1-C4
  • alkyl groups are generally understood to mean straight-chain, branched or cyclic alkyl groups. It is e.g. around methyl, ethyl, propyl, i-propyl, butyl, i-butyl, tert-butyl, amyl, tert-amyl (1,1-dimethylpropyl), 1,1,3,3-tetramethylbutyl, hexyl, 1- Methylpentyl, neopentyl, 1-, 2- or 3-methylhexyl, heptyl, n-octyl, tert.
  • alkyl radicals can be substituted, e.g. by hydroxy, alkoxy, with 1 to 4 carbon atoms, especially methoxy, cyano or phenyl.
  • Halogen such as fluorine, chlorine or bromine, or -CO-U, where U is alkyl having 1 to 6 carbon atoms or phenyl, are suitable as further substituents.
  • Suitable alkenyl radicals are those radicals which are derived from the alkyl radicals listed above by replacing at least one single bond with a double bond.
  • Suitable residues are e.g. Ethenyl or propenyl.
  • Suitable alkoxy radicals are e.g. Methoxy, ethoxy, propoxy, iso-propoxy, n-butoxy, i-butoxy or tert-butoxy.
  • Suitable substituted alkyl radicals are: methoxymethyl, ethoxymethyl, ethoxyethyl, ethoxypropyl, n-propoxymethyl, iso-propoxymethyl, butoxymethyl, butoxyethyl, butoxypropyl, ethoxypentyl, methoxybutyl, ethoxypentyl, 2-hydroxyethoxypentyl, cyanoethyl, hydroxyethyl.
  • the alkylene radicals B can also be straight-chain or branched or else substituted.
  • Ethylene, 1,3-propylene, 1,2-propylene, 1,2-butylene, 1,6-hexylene, 2-hydroxy-1,3-propylene or 2-chloro-1,3-propylene are possible.
  • phenyl radicals are generally to be understood as meaning unsubstituted or substituted phenyl radicals.
  • substituents are C1-C4-alkyl, C1-C4-alkoxy, bromine, chlorine, nitro or C1-C4-alkylcarbonylamino into consideration.
  • Halogen in this application generally means fluorine, bromine or especially chlorine.
  • Z means a direct bond or a bridge member from the series are preferred if the bond to the radical A takes place via a carbon atom of this radical. If the radical A has a hetero atom via which the bond with the remaining dye molecule of the formula (1) takes place, then Z preferably represents a direct bond.
  • Preferred radicals A are the radicals of the formulas These radicals can also carry the substituents customary in disperse dyes, for example C1-C4-alkyl, C1-C4-alkoxy, halogen or nitro.
  • X are hydrogen, methyl, methoxy, chlorine or bromine, with hydrogen and methyl being particularly preferred.
  • Y is preferably chlorine, methyl, methoxy, methoxyethyl or methoxyethoxy or especially hydrogen.
  • R is C1-C4-alkyl, which is optionally substituted by hydroxy, C1-C4-alkoxy or phenyl. In particularly preferred compounds of formula (1), R is methyl, ethyl or benzyl.
  • R and Y together with the nitrogen atom and the two carbon atoms connecting them, can form a 5- or 6-membered ring which can optionally contain an oxygen atom as a further heteroatom.
  • Suitable substituents for these rings are e.g. Hydroxy, methyl, methoxy, chlorine or phenyl.
  • B preferably represents a straight-chain or branched alkylene radical having 2 to 4 carbon atoms, which is optionally substituted by hydroxy.
  • the disperse dyes of the formula (1) in which B is ethylene or 1,3-propylene are particularly preferred.
  • the dyes of the formula are above all of interest in what X1 is hydrogen or methyl R1 is methyl, ethyl or benzyl Z1 the direct bond, -O-, -S- or A1 is a radical of the formula is.
  • the compounds of the formula (1) are prepared in a manner known per se, for example by using a compound of the formula with tetracyanethylene, or by using a compound of formula with a cyanide and then with an oxidizing agent.
  • the compounds of the formulas (3) and (4) are known or can be obtained in a manner known per se.
  • the compounds of the formula (3) can be obtained, for example, by reacting a compound of the formula Hal - B - Z - A with an aniline derivative of the formula wherein the compounds of formula (5), for example, by reacting a compound of formula with a compound of the formula receives.
  • A, Z, B, X, Y and R have the meaning given under the formula (1) and Hal means chlorine or bromine, where the two halogen atoms can be the same or different.
  • the compounds of the formulas (7) and (8) are known or can be prepared in a known manner.
  • the reaction of the compound (7) with the compound (8) is preferably carried out in an inert organic solvent and in the presence of a base.
  • Suitable inert organic solvents are, for example, compounds with a boiling point above 100 ° C., such as alcohols, ethers, esters, nitrobenzene, halogenobenzene, toluene, xylenes etc. are particularly suitable higher-boiling alcohols, such as tert-butanol, and ethers of polyhydric alcohols, for example diethylene glycol monoethyl ether or monomethyl ether, and the corresponding diethers.
  • Components (7) and (8) can be used in a stoichiometric ratio, but an excess of one of the components, preferably compound (8), often proves to be more favorable.
  • the reaction temperature is approximately between 80 and 150 ° C, preferably between 100 and 130 ° C and the reaction time is, depending on the temperature and reactants, about 1 to 20 hours.
  • any component (8) which may be used in excess is removed and the compound of the formula (5) obtained is then reacted with an aniline derivative of the formula (6).
  • This reaction is also preferably carried out in one of the abovementioned solvents.
  • the temperature is usually above 100 ° C, in particular between 120 and 200 ° C and especially between 140 and 180 ° C.
  • the components (5) and (6) can be used in a stoichiometric ratio, but normally the more accessible component, usually the aniline derivative (6), is used in excess, for example in a 10% excess.
  • the mixture is worked up in the customary manner, for example by removing the excess of component (6) and the solvent and, if appropriate, cleaning the residue, for example by recrystallization.
  • Both the reaction of compounds (7) and (8) and the reaction of compounds (5) and (6) are carried out in the presence of a base, both organic and inorganic bases being suitable, for example pyridine, piperidine, triethylamine , Sodium or potassium carbonate or bicarbonate. This base is generally used in a slight excess, for example in a 10% excess.
  • the entire preparation of the compound (3) can also be carried out as a so-called one-pot reaction by using the same solvent for the two reaction steps and not isolating the compound (5).
  • the compounds of formula (4) are e.g. obtained by first preparing a compound of formula (3) under the known conditions of Vilsmeier synthesis with e.g. POCl3 and dimethylformamide or phosgene and dimethylformamide and then reacted with malodinitrile.
  • the compounds of the formula (3) are reacted with tetracyanethylene in a manner known per se, preferably in an inert solvent at a temperature between about 20 and 100 ° C., the reaction components being used in approximately equivalent amounts.
  • the compounds of the formula (4) are also reacted with a cyanide and then with an oxidizing agent in a manner known per se.
  • the reaction is preferably carried out as a one-pot reaction, i.e. without isolation of the intermediate, and also in an inert solvent.
  • Potassium or sodium cyanide is primarily used as the cyanide and bromine in particular as the oxidizing agent.
  • the reaction with the cyanide is preferably carried out at about 20 to 100 ° C and the reaction with the oxidizing agent at about 0 to 20 ° C.
  • Halogen compounds such as chloroform or chlorobenzene, ethers, aromatic compounds such as benzene, toluene or xylene, but especially tetrahydrofuran or dimethylformamide.
  • the isolation of the dyes of formula (1) takes place e.g. by pouring the reaction solutions into ice water, filtering off the excreted dye, possibly washing and drying.
  • the compounds of formula (1) according to the invention can be used as dyes for dyeing and printing semi-synthetic and in particular synthetic hydrophobic fiber materials, especially textile materials. Textile materials from blended fabrics which contain such semi-synthetic or synthetic hydrophobic textile materials can also be dyed or printed with the aid of the compounds according to the invention.
  • cellulose 2 1/2 acetate and cellulose triacetate are particularly suitable.
  • Synthetic hydrophobic textile materials consist primarily of linear, aromatic polyesters, for example those made of terephthalic acid and glycols, especially ethylene glycol or condensation products made of terephthalic acid and 1,4-bis (hydroxymethyl) cyclohexane; from polycarbonates, e.g. those from ⁇ , ⁇ -dimethyl-4,4'-dihydroxy-diphenylmethane and phosgene, from fibers based on polyvinyl chloride and polyamide.
  • polyester fiber materials are dyed in the exhaust process from aqueous dispersion in the presence of customary anionic or nonionic dispersants and, if appropriate, customary swelling agents (carriers) at temperatures between 80 and 140 ° C.
  • Cellulose-2 1/2 acetate is preferably dyed between about 65 to 85 ° C and cellulose triacetate at temperatures up to 115 ° C.
  • the new dyes do not or only slightly stain the wool and cotton present in the dyebath (very good reserve), so that they can also be used well for dyeing polyester / wool and polyester / cellulose fiber blended fabrics.
  • the dyes according to the invention are particularly suitable for dyeing by the thermosol process.
  • the textile material mentioned can be in a wide variety of processing forms, such as as fiber, thread or fleece, as woven or knitted fabric.
  • the dyes according to the invention are converted into a dye preparation before they are used.
  • the dye is ground so that its average particle size is between 0.01 and 10 microns.
  • the grinding can take place in the presence of dispersants.
  • the dried dye is ground with a dispersant or in paste form with a dispersant kneaded and then dried in vacuo or by atomization. With the preparations so preserved, you can dye and print after adding water.
  • the usual thickeners will be used for printing, e.g. modified or unmodified natural products, for example alginates, British gum, gum arabic, crystal gum, locust bean gum, tragacanth, carboxymethyl cellulose, hydroxyethyl cellulose, starch or synthetic products, for example polyacrylamides, polyacrylic acid or their copolymers or polyvinyl alcohols.
  • modified or unmodified natural products for example alginates, British gum, gum arabic, crystal gum, locust bean gum, tragacanth, carboxymethyl cellulose, hydroxyethyl cellulose, starch or synthetic products, for example polyacrylamides, polyacrylic acid or their copolymers or polyvinyl alcohols.
  • the dyes according to the invention give the materials mentioned, especially the polyester material, level orange or red shades of very good fastness to use, such as, above all, good lightfastness, heat-setting, pleating, chlorine and wet fastness such as water, sweat and washfastness; the colorations are also characterized by good pH stability and very good fastness to rubbing. Very strong colorations are also achieved. Of particular note is the good thermomigration fastness of the dyeings obtained.
  • the dyes according to the invention can also be used well to produce mixed shades together with other dyes. Mixtures of the dyes according to the invention can of course also be used with one another.
  • the abovementioned use of the azo compounds of the formula (1) according to the invention is also an object of the present invention, as is a process for dyeing or printing semi-synthetic or synthetic hydrophobic fiber material, in particular textile material, which consists in one or more compounds of the formula ( 1) to apply to the material mentioned or to incorporate it into it.
  • the hydrophobic fiber material mentioned is preferably textile polyester material.
  • Another object of the invention is the hydrophobic fiber material, preferably polyester textile material, dyed or printed by the method mentioned.
  • JP-A-59-129264 already describes tricyanostyryl dyes which, however, do not contain the rest A of the dyes according to the invention.
  • the starting connection is made as follows: 19.8 g of 4-hydroxyazobenzene are dissolved in 100 ml of diethylene glycol monoethyl ether, and 12.8 g of soda and 52.5 ml of 1,2-dibromoethane are added. The mixture is heated to about 116 ° C. and stirred at this temperature for 2 hours. The excess dibromoethane is then removed by steam distillation and then the water by distillation at about 110 ° C in a vacuum. A suspension is obtained containing about 26 g of an orange-red powder of the formula
  • 1 part of the dry, coupage-free dye according to Example 1 is mixed in a sand mill together with 2 parts of dinaphthyl methane disulfonate (Na salt), 34 parts of quartz sand and 17 parts of water, and the mixture is ground until a particle size of about 2 ⁇ or less is achieved is.
  • the resulting suspension is separated from the sand and then forms a stable liquid formulation.
  • it can also be subjected to spray drying, a powdery dyeing preparation being obtained.
  • Polyethylene glycol terephthalate fabric is impregnated on a padder at 40 ° with a liquor of the following composition: 20 parts of the dye preparation obtained according to Example 14 finely dispersed in 10 parts of sodium alginate, 20 parts of octylphenol polyglycol ether and 930 parts water.
  • the dyed goods are rinsed with water, soaped or reductively cleaned and dried. A brilliant, lightfast red coloration is obtained, which is characterized above all by good thermomigration fastness.
  • the dyeing is then rinsed and aftertreated with aqueous sodium hydroxide solution and a dispersant. This gives a light and sublimation-resistant red color.
  • Example 5 1 part of the dye obtained in Example 5 is wet-ground with 2 parts of a 50% aqueous solution of the sodium salt of dinaphthylmethane disulfonic acid and dried.
  • This dye preparation is stirred with 40 parts of a 10% aqueous solution of the sodium salt of N-benzylheptadecylbenzimidazole disulfonic acid and 4 parts of a 40% acetic acid solution are added.
  • a dye bath of 4000 parts is prepared from this by dilution with water.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Coloring (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)
  • Optical Filters (AREA)

Claims (20)

1. Colorants dispersés de formule
Figure imgb0049
 dans laquelle
X représente un atome d'hydrogène, un groupe alkyle en C₁₋₄, alcoxy en C₁₋₄, ou un atome d'halogène,
Y représente un atome d'hydrogène ou d'halogène, un groupe alkyle en C₁₋₄, alcoxy en C₁₋₄, alcoxy(C₁₋₄)-alkyle(C₁₋₄) ou alcoxy(C₁₋₄)-alcoxy(C₁₋₄),
R représente un atome d'hydrogène, un groupe alkyle en C₁₋₁₂, alcényle en C₂₋₁₂ ou phényle, ou bien
Y et R forment, ensemble avec l'atome d'azote et les deux atomes de carbone qui les relient, un cycle à 5 ou 6 chaînons, et
B représente un reste alkylène en C₂₋₆ linéaire ou ramifié,
Z représente un pont de formule -O-, -S-, -NH-, -C(=O)-NH-, -O-C(=O)-, NH-C(=O)-
ou une liaison directe, et
A représente un reste de formule
Figure imgb0050
Figure imgb0051
 ces restes pouvant encore être substitués par des groupes alkyle en C₁₋₄, alcoxy en C₁₋₄, halogène ou nitro.
2. Colorants selon la revendication 1, dans lesquels X est hydrogène, méthyle, méthoxy, chloro ou bromo.
3. Colorants selon la revendication 2, dans lesquels X est hydrogène ou méthyle.
4. Colorants selon une des revendications 1 à 3, dans lesquels Y est hydrogène, chloro, méthyle, méthoxy, méthoxyéthyle ou méthoxyéthoxy.
5. Colorants selon la revendication 4, dans lesquels Y est hydrogène.
6. Colorants selon une des revendications 1 à 5, dans lesquels R représente un groupe alkyle en C₁₋₄, qui peut être substitué par hydroxy, alcoxy en C₁₋₄ ou phényle.
7. Colorants selon la revendication 6, dans lesquels R est méthyle, éthyle ou benzyle.
8. Colorants selon une des revendications 1 à 3, dans lesquels R et Y forment, ensemble avec l'atome d'azote et les deux atomes de carbone qui les relient, un cycle à 6 chaînons, non substitué ou porteur de 1 à 3 groupes méthyle.
9. Colorants selon une des revendications 1 à 8, dans lesquels B représente un groupe alkylène, non substitué ou substitué par hydroxy.
10. Colorants selon la revendication 9, dans lesquels B est éthylène ou 1,3-propylène.
11. Colorants selon une des revendications 1 à 10, dans lesquels Z est -O- ou -O-C(=O)-.
12. Colorants selon une des revendications 1 à 11, dans lesquels A représente un reste de formule.
Figure imgb0052
 ces restes pouvant encore être substitués par des groupes alkyle en C₁₋₄, alcoxy en C₁₋₄, halogène ou nitro.
13. Colorants de formule
Figure imgb0053
 dans laquelle
X¹ est hydrogène ou méthyle,
R¹ est méthyle, éthyle ou benzyle,
Z¹ est la liaison directe, -O-, -S- ou -O-C(=O)-,
A¹ représente un reste de formule
Figure imgb0054
14. Procédé de préparation de colorants dispersés de formule (1) selon la revendication 1, caractérisé en ce que l'on fait réagir un composé de formule
Figure imgb0055
 avec du tétracyanoéthylène, ou en ce qu'on fait réagir un composé de formule
Figure imgb0056
 avec un cyanure et ensuite avec un oxydant.
15. Utilisation des colorants dispersés de la revendication 1, pour la teinture ou l'impression de matière fibreuse hydrophobe semi-synthétique ou synthétique, en particulier de matière textile.
16. Utilisation selon la revendication 15 pour la teinture ou l'impression de matière textile en fibres de polyester.
17. Procédé de teinture ou d'impression d'une matière fibreuse hydrophobe semi-synthétique ou synthétique, en particulier d'une matière textile, caractérisé en ce que l'on dépose un ou plusieurs des composés définis dans la revendication 1 sur l'ensemble de la matière ou bien qu'on incorpore ce ou ces composés à ladite matière.
18. Procédé selon la revendication 17, dans lequel la matière fibreuse hydrophobe, de préférence matière textile, est à base de fibres de polyester.
19. Matière teinte ou imprimée selon la revendication 17 ou 18.
20. Préparations de colorants, renfermant un colorant selon la revendication 1 et les additifs usuels pour colorants dispersés.
EP88810156A 1987-03-19 1988-03-14 Colorants de dispersion contenant un groupement tricyanovinyle Expired - Lifetime EP0284560B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
CH1050/87 1987-03-19
CH105087 1987-03-19
CH509187 1987-12-29
CH5091/87 1987-12-29

Publications (3)

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EP0284560A2 EP0284560A2 (fr) 1988-09-28
EP0284560A3 EP0284560A3 (en) 1989-01-04
EP0284560B1 true EP0284560B1 (fr) 1992-03-04

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US (1) US4914190A (fr)
EP (1) EP0284560B1 (fr)
JP (1) JPS63254168A (fr)
KR (1) KR880011287A (fr)
DE (1) DE3868656D1 (fr)

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Publication number Priority date Publication date Assignee Title
US5218136A (en) * 1987-12-28 1993-06-08 Sumitomo Chemical Company, Limited Styryl compounds, process for preparing the same and photoresist compositions comprising the same
EP0351367A3 (fr) * 1988-07-11 1991-09-18 Ciba-Geigy Ag Colorants de dispersion contenant un groupement tricyanvinyle
EP0363904B1 (fr) * 1988-10-11 1995-04-05 Sumitomo Chemical Company Limited Colorants de dispersion monoazo, leur préparation et leur emploi
EP0378510B1 (fr) * 1989-01-13 1996-09-18 Ciba-Geigy Ag Colorants de dispersion
DE4004613A1 (de) * 1990-02-15 1991-08-22 Basf Ag Bichromophore cyanogruppen aufweisende methinfarbstoffe und ein verfahren zu ihrer uebertragung
DE4042194A1 (de) * 1990-12-29 1992-07-02 Basf Ag Styrolderivate

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US2749229A (en) * 1952-05-06 1956-06-05 Ethyl Corp Plant growth regulation with chlorophenyl cyanoacrylic acids and derivatives
US2762833A (en) * 1953-09-28 1956-09-11 Du Pont Process for preparing tricyanovinylphenols
US2889335A (en) * 1955-01-14 1959-06-02 Du Pont Process for preparing c-tricyanovinyl compounds and a new class of tricyanovinyl aromatic compounds adapted for use as dyes
US2849447A (en) * 1955-09-19 1958-08-26 Gen Aniline & Film Corp Nitro diarylamine methine dyes
US3240783A (en) * 1963-01-18 1966-03-15 Eastman Kodak Co Cyanomethylidene quinolines
GB1110714A (en) * 1966-04-13 1968-04-24 Ici Ltd New styryl dyestuffs
US4035380A (en) * 1966-08-29 1977-07-12 Ciba-Geigy Ag Certain benzazol-2-ylthio compounds
DE2059291A1 (de) * 1970-12-02 1972-06-08 Basf Ag Styrylfarbstoffe
US3890367A (en) * 1971-10-18 1975-06-17 Gulf Research Development Co 3,5-Tert. butyl-4-(2,4-dichlorophenylcarbamyloxy) benzylidenemalonitrile
US3926945A (en) * 1972-05-16 1975-12-16 Gaf Corp 2,4-Dicyano butylamino-substituted monoazo dyestuffs
DD111920A5 (fr) * 1973-04-04 1975-03-12
FR2280672A1 (fr) * 1974-08-02 1976-02-27 Ugine Kuhlmann Copolymeres structurellement colores a base de colorants cyanovinyl-azoiques
DE2542376C2 (de) * 1974-10-04 1984-05-17 Sandoz-Patent-GmbH, 7850 Lörrach Organische Verbindungen
DE2714653C3 (de) * 1977-04-01 1980-10-30 Bayer Ag, 5090 Leverkusen Kationische Styrylfarbstoffe und Verfahren zum Färben mit diesen Farbstoffen
JPS59129264A (ja) * 1983-01-12 1984-07-25 Sumitomo Chem Co Ltd トリシアノスチリル化合物およびそれを用いる染色または着色法
JPS59129263A (ja) * 1983-01-12 1984-07-25 Sumitomo Chem Co Ltd トリシアノスチリル化合物およびそれを用いる染色または着色方法
DE3417840A1 (de) * 1983-05-17 1984-11-22 Ciba-Geigy Ag, Basel Tetrazolverbindungen

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Publication number Publication date
KR880011287A (ko) 1988-10-27
EP0284560A2 (fr) 1988-09-28
EP0284560A3 (en) 1989-01-04
US4914190A (en) 1990-04-03
DE3868656D1 (de) 1992-04-09
JPS63254168A (ja) 1988-10-20

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